ARTO
Head of Manufacturing Science and Technology (MSAT)
ARTO, Oklahoma City, Oklahoma, United States, 73116
Head of Manufacturing Science and Technology (MSAT)
Location: Oklahoma City Metropolitan Area
Biopharmaceuticals | Large Molecules | GMP Manufacturing
About the Role A leading biopharmaceutical manufacturing organization is seeking an experienced
Head of Manufacturing Science & Technology (MST)
to lead and develop its MST function. This role is critical to supporting GMP manufacturing operations, driving process excellence, and ensuring successful technology transfer and scale-up for large molecule programs.
The successful candidate will provide technical leadership across production support, process optimization, and regulatory readiness, while building and mentoring a high‑performing MST team.
Key Responsibilities
Develop and execute annual MST plans aligned with overall business strategy, operational goals, and regulatory requirements
Lead and manage the MST team, providing technical oversight and day‑to‑day support to GMP manufacturing operations
Serve as the technical escalation point for manufacturing challenges, ensuring timely root‑cause analysis and resolution
Drive process development, optimization, and continuous improvement to enhance process robustness, efficiency, and compliance
Lead technology transfer and scale‑up activities, ensuring reproducibility and successful integration into commercial manufacturing
Support internal and external audits and regulatory inspections, ensuring processes and documentation meet GMP standards
Establish, optimize, and maintain laboratory systems, procedures, and quality standards to ensure reliable and compliant data generation
Develop, coach, and mentor MST team members to strengthen technical capability, leadership, and overall performance
Qualifications
Master’s degree or higher in Biotechnology, Pharmaceutical Sciences, Chemical Engineering, or a related discipline
Minimum of 10 years’ experience in the biopharmaceutical industry, with at least 5 years in a people management role
Strong expertise in large molecule development, technology transfer, process optimization, and GMP manufacturing
Proven ability to troubleshoot complex technical issues in a production environment
Excellent communication, problem‑solving, and cross‑functional collaboration skills
Strong leadership skills with a demonstrated ability to develop technical teams
Fluent in English (written and spoken)
Preferred Experience
Background within a CDMO or contract manufacturing environment
Familiarity with U.S. FDA and EU regulatory expectations
Why This Role This is a senior leadership opportunity to shape manufacturing science and technology strategy within a growing biopharmaceutical operation, offering significant influence over process performance, regulatory success, and team development.
Seniority level
Director
Employment type
Full‑time
Job function
Manufacturing and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Biopharmaceuticals | Large Molecules | GMP Manufacturing
About the Role A leading biopharmaceutical manufacturing organization is seeking an experienced
Head of Manufacturing Science & Technology (MST)
to lead and develop its MST function. This role is critical to supporting GMP manufacturing operations, driving process excellence, and ensuring successful technology transfer and scale-up for large molecule programs.
The successful candidate will provide technical leadership across production support, process optimization, and regulatory readiness, while building and mentoring a high‑performing MST team.
Key Responsibilities
Develop and execute annual MST plans aligned with overall business strategy, operational goals, and regulatory requirements
Lead and manage the MST team, providing technical oversight and day‑to‑day support to GMP manufacturing operations
Serve as the technical escalation point for manufacturing challenges, ensuring timely root‑cause analysis and resolution
Drive process development, optimization, and continuous improvement to enhance process robustness, efficiency, and compliance
Lead technology transfer and scale‑up activities, ensuring reproducibility and successful integration into commercial manufacturing
Support internal and external audits and regulatory inspections, ensuring processes and documentation meet GMP standards
Establish, optimize, and maintain laboratory systems, procedures, and quality standards to ensure reliable and compliant data generation
Develop, coach, and mentor MST team members to strengthen technical capability, leadership, and overall performance
Qualifications
Master’s degree or higher in Biotechnology, Pharmaceutical Sciences, Chemical Engineering, or a related discipline
Minimum of 10 years’ experience in the biopharmaceutical industry, with at least 5 years in a people management role
Strong expertise in large molecule development, technology transfer, process optimization, and GMP manufacturing
Proven ability to troubleshoot complex technical issues in a production environment
Excellent communication, problem‑solving, and cross‑functional collaboration skills
Strong leadership skills with a demonstrated ability to develop technical teams
Fluent in English (written and spoken)
Preferred Experience
Background within a CDMO or contract manufacturing environment
Familiarity with U.S. FDA and EU regulatory expectations
Why This Role This is a senior leadership opportunity to shape manufacturing science and technology strategy within a growing biopharmaceutical operation, offering significant influence over process performance, regulatory success, and team development.
Seniority level
Director
Employment type
Full‑time
Job function
Manufacturing and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr